Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Stanka, Romac"'
Autor:
Galina Stevanović, Stanka Romac, Miljana Kecmanovic, Milica Keckarević-Marković, Nebojša Jović, Dušan Keckarević
Publikováno v:
The Application of Clinical Genetics
Lafora disease (LD) is a fatal neurodegenerative disorder caused by loss-of-function mutations in either laforin glycogen phosphatase gene (EPM2A) or malin E3 ubiquitin ligase gene (NHLRC1). LD is associated with gradual accumulation of Lafora bodies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a8b2f6a5da49960349fe75031bb7aad
http://europepmc.org/articles/PMC4859416
http://europepmc.org/articles/PMC4859416
Autor:
S. Cidilko, N. Vucic, Zorana Nikolic, Goran Brajušković, Snežana Cerović, Nenad Filipovic, D. Savic Pavicevic, V. Vukotic, Stanka Romac
Publikováno v:
Experimental and Molecular Pathology. 99:145-150
Due to their potentially functional significance, genetic variants within microRNA genes have been recognized as candidates for cancer-related genetic biomarkers. Among the most extensively studied so far are rs3746444, rs11614913 and rs895819. Never
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::633ab03084bc9a630eccdefdbb7d26b7
https://doi.org/10.1016/j.yexmp.2015.06.009
https://doi.org/10.1016/j.yexmp.2015.06.009
Autor:
Stanka Romac, P. Ignjatovic, Miljana Kecmanovic, Dušan Keckarević, Galina Stevanović, Nebojša Jović, Milica Keckarević-Marković
Publikováno v:
Clinical Genetics. 89:104-108
Lafora disease (LD) is an autosomal recessive, progressive disorder characterized by myoclonus and seizures, inexorable neurologic deterioration, cognitive decline and poor prognosis. LD is caused by mutations either in the EPM2A or in NHLRC1 genes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::173098bbefc50775d1935a30045e0e31
https://doi.org/10.1111/cge.12570
https://doi.org/10.1111/cge.12570
Publikováno v:
Public Health Genomics. 18:283-298
Background and Aims: A large number of studies have investigated the association between the potentially functional genetic variant rs2910164 located in the hsa-miR-146a gene and susceptibility to various types of cancer. Nevertheless, the results ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad293f5febfb53a90071b7b61d2812ac
https://doi.org/10.1159/000438695
https://doi.org/10.1159/000438695
Publikováno v:
Clinical and Translational Science. 8:23-31
Several variants within gene-encoding endothelial isoform of nitric oxide synthase have been reported to confer prostate cancer (PCa) susceptibility and/or progression. Nevertheless, studies referring to this issue have yielded inconsistent results.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f49815d113bc0b574e336e8b7cdcc2a7
https://doi.org/10.1111/cts.12203
https://doi.org/10.1111/cts.12203
Autor:
Dusanka Savic-Pavicevic, Stefan Prekovic, Ana S. Branković, S. Tomovic, Zorana Nikolic, Goran Brajušković, V. Vukotic, Natasa Filipovic, Stanka Romac, Snežana Cerović
Publikováno v:
Clinical and Translational Science. 7:307-313
This study aimed to evaluate possible association between genotypes and alleles of two 17q12 polymorphisms (rs3760511 and rs7501939) and prostate cancer (PCa) risk and progression. Two hundred seventy-one patients with PCa, 261 patients with benign p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1825141be175d484b0ddbf9e8734b17c
https://doi.org/10.1111/cts.12130
https://doi.org/10.1111/cts.12130
Autor:
Aleksandar J. Ristić, Dušan Keckarević, Milica Keckarević-Marković, Miljana Kecmanovic, Dragoslav Sokić, Marko Ercegovac, Stanka Romac
Publikováno v:
International Journal of Neuroscience. 124:102-109
Unverricht-Lundborg disease (ULD) is an autosomal recessive disorder caused by dodecamer repeat expansion in the promoter region of the cystatin B (CSTB) gene in approximately 90% of the disease alleles worldwide. This study presents results of genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6eb07f1e072ecca8c6c4391d5af2f85c
https://doi.org/10.3109/00207454.2013.828723
https://doi.org/10.3109/00207454.2013.828723
Autor:
Snezana Cerovic, Dusanka Savic-Pavicevic, S. Tomovic, Zorana Nikolic, Goran Brajušković, A. Kojic, Natasa Filipovic, Stanka Romac, V. Vukotic
Publikováno v:
Archives of Biological Sciences, Vol 65, Iss 2, Pp 475-486 (2013)
Prostate cancer (PCa) is the second most commonly diagnosed cancer among men worldwide. Despite its high incidence rate, the molecular basis of PCa onset and its progression remains little understood. Genome-wide association studies (GWAS) have great
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d1de9f2133b9c0f8d52ec898f79df42
https://doi.org/10.2298/abs1302475b
https://doi.org/10.2298/abs1302475b
Autor:
Milica Gagic, Miljana Kecmanovic, Milica Marković, Vedrana Milic-Rasic, Jelena Dackovic, Jelena Mladenović, Dušan Keckarević, Stanka Romac
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 54
Background Charcot-Marie-Tooth type 1A (CMT1A) is the most common type of hereditary motor and sensory neuropathies (HMSN), caused by the duplication of the 17p11.2 region that includes the PMP22 gene. Reciprocal deletion of the same region is the ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::919ebd49c859bcf03964294c5baa2a0f
https://doi.org/10.1515/cclm-2015-0602
https://doi.org/10.1515/cclm-2015-0602
Publikováno v:
Archives of Biological Sciences, Vol 63, Iss 3, Pp 527-535 (2011)
Apoptosis or programmed cell death is a genetically regulated process of cellular suicide. Apoptosis has been implicated in a wide range of pathological conditions, and mutations in apoptotic genes play important roles in the process of malignant tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b31dd99456616e69a1adccd5a412c0c7
https://doi.org/10.2298/abs1103527b
https://doi.org/10.2298/abs1103527b